| Morchella sextelata | |
|---|---|
 | |
Scientific classification  | |
| Domain: | Eukaryota |
| Kingdom: | Fungi |
| Division: | Ascomycota |
| Class: | Pezizomycetes |
| Order: | Pezizales |
| Family: | Morchellaceae |
| Genus: | Morchella |
| Species: | M. sextelata |
| Binomial name | |
| Morchella sextelata M.Kuo (2012) | |
Morchella sextelata is a species of ascomycete fungus in the family Morchellaceae. Described as new to science in 2012, it is found in North America (in Washington, Idaho, Montana, Wyoming, New Mexico, and Yukon Territory). It has also been found in China, although it is not known if this is a result of an accidental introduction or natural dispersion. The fruit bodies have a roughly conical cap up to 7.5 cm (3 in) tall and 5 cm (2 in) wide, with a surface of mostly vertically arranged pits. The cap is initially yellowish to brownish, but it darkens to become almost black in maturity. The stipe is white and hollow, measuring 2–5 cm (0.8–2.0 in) high by 1–2.2 cm (0.4–0.9 in) wide.
Morchella sextelata is one of four species of wildfire-adapted morels in western North America, the others being M. capitata, M. septimelata, and M. tomentosa. M. sextelata cannot be reliably distinguished from M. septimelata without the use of DNA analysis.
Taxonomy
Morchella sextelata was originally identified as phylogenetic species "Mel-6" in the species-rich Elata clade (brown morels) elucidated by microbiologist Kerry O'Donnell and colleagues in a 2011 publication. The specific epithet sextelata alludes to this preliminary name. Although M. sextelata is not distinguishable from Morchella septimelata on physical or ecological characteristics, they are clearly genetically distinct species, and can be differentiated by comparing DNA sequences or with restriction fragment length polymorphism analysis.[1] Allopatric speciation is thought to have been the driving evolutionary force that caused M. sextelata to diverge from its ancestors roughly 25 million years ago.[2] The original specimens collected were obtained as part of the Morel Data Collection Project,[2] a research effort designed to improve the understanding of North American morels.[3]
Description
The fruit bodies of Morchella sextelata are 4–10.5 cm (1.6–4.1 in) high with a conical cap that is 2.5–7.5 cm (1.0–3.0 in) high and 2–5 cm (0.8–2.0 in) wide at the widest point. The cap surface features pits and ridges, formed by the intersection of 12–20 primary vertical ridges and frequent shorter, secondary vertical ridges, with occasional sunken, horizontal ridges. The cap is attached to the stipe with a sinus about 2–4 mm deep and 2–4 mm wide. The ridges are smooth or very finely tomentose (covered with densely matted filaments). They are initially colorless, becoming pale tan, then dark grayish brown in maturity, eventually darkening to nearly black. They are flattened when young but sometimes become sharpened or eroded in maturity. The pits are somewhat elongated vertically. They are smooth, brownish to yellowish tan to pinkish to buff.[1]
The whitish to pale brownish stipe is 2–5 cm (0.8–2.0 in) long by 1.0–2.2 cm (0.4–0.9 in) wide and is roughly equal in width throughout its length, or sometimes slightly club-shaped near the base. Its surface is either smooth or covered with whitish granules. The flesh is whitish, measuring 1–2 mm thick in the hollow cap; it may become layered and chambered in the base of the stipe. The sterile inner surface of the cap is whitish and pubescent (covered with short, soft "hair").[1]
The ascospores of M. sextelata are elliptical and smooth, typically measuring 18–25 by 10–16 µm. Asci (spore-bearing cells) are eight-spored, hyaline (translucent), cylindrical, and measure 200–325 by 5–25 µm. Paraphyses are cylindrical, septate, and measure 175–300 by 2–15 µm. Their tips are variably shaped, from rounded, to club-shaped, to fuse-shaped. The contents of the paraphyses are hyaline (translucent) to faintly brownish in dilute potassium hydroxide (KOH). Hyphae on the sterile cap ridges are septate and measure 50–180 by 5–25 µm. The terminal cells are variably shaped (similar to the paraphyses), and have brownish contents in KOH.[1]
North American Morchella are generally considered choice edibles,[4] but the edibility of M. sextelata was not mentioned in its original description.[1]
Similar species
Morchella sextelata is morphologically indistinguishable from several other morel species in the M. elata clade, including M. septimelata, M. brunnea, M. angusticeps, and M. septentrionalis. M. septimelata can be distinguished from these latter three lookalikes by habitat or distribution: M. brunnea is found in non-burned forests of western North America; M. angusticeps is found east of the Rocky Mountains; and M. septentrionalis is restricted to a northern distribution (about 44°N northward) in eastern North America. M. septimelata, however, also grows in burn sites and so is both morphologically and ecologically indistinguishable from M. sextelata. Although there are subtle differences in the structure of the sterile ridges between the species, the authors were not confident that enough specimens had been examined to establish that these differences were consistent.[1]
Habitat, distribution, and ecology
Morchella sextelata may be either saprobic or mycorrhizal at different times in its life cycle.[5] Its fruit bodies grow in partially burned conifer forests, particularly those dominated by Douglas fir (Pseudotsuga menziesii) and ponderosa pine (Pinus ponderosa). They tend to appear in great numbers the year immediately following fire and appear in decreasing frequency in successive years. Fruiting occurs from April through July, at elevations between 1,000 and 1,500 m (3,300 and 4,900 ft). The distribution includes Washington, Idaho, Montana, Wyoming, and Yukon Territory.[1] M. sextelata has also been found in China, but it remains unclear whether dispersal between these distant locations occurred naturally or through accidental introduction by humans.[6]
Morchella sextelata, identified as phylogenetic species "Mel-6", has been shown to colonize the non-native species Bromus tectorum (cheatgrass) as an endophyte, increasing the overall growth of the grass, as well as the abundance of seeds and their tolerance to extreme heat (60–65 °C (140–149 °F)). This has been hypothesized to be a contributing factor in the success of cheatgrass as an invasive species in western North America.[7]
References
- 1 2 3 4 5 6 7 Kuo M, Dewsbury DR, O'Donnell K, Carter MC, Rehner SA, Moore JD, Moncalvo JM, Canfield SA, Stephenson SL, Methven AS, Volk TJ (2012). "Taxonomic revision of true morels (Morchella) in Canada and the United States". Mycologia. 104 (5): 1159–77. doi:10.3852/11-375. PMID 22495449. S2CID 45219627.
- 1 2 O'Donnell K, Rooney AP, Mills GL, Kuo M, Weber NS, Rehner SA (2011). "Phylogeny and historical biogeography of true morels (Morchella) reveals an early Cretaceous origin and high continental endemism and provincialism in the Holarctic". Fungal Genetics and Biology. 48 (3): 252–65. doi:10.1016/j.fgb.2010.09.006. PMID 20888422.
- ↑ Kuo M. (December 2012). "Morel Data Collection Project Records". MushroomExpert.com. Retrieved 2014-10-05.
- ↑ Kuo M. (2005). Morels. Ann Arbor, Michigan: University of Michigan Press. ISBN 978-0-472-03036-1.
- ↑ Kuo M. (October 2010). "Morchella sextelata". MushroomExpert.com. Retrieved 2014-10-05.
- ↑ Du X-H; Zhao Q; O’Donnell K; Rooney AP; Yang ZL. (2012). "Multigene molecular phylogenetics reveals true morels (Morchella) are especially species-rich in China". Fungal Genetics and Biology. 49 (6): 455–69. doi:10.1016/j.fgb.2012.03.006. PMID 22503770.
- ↑ Baynes MA; Newcombe G; Dixon L; Castlebury L; O’Donnell K. (2012). "A novel plant-fungal mutualism associated with fire" (PDF). Fungal Biology. 116 (1): 133–44. doi:10.1016/j.funbio.2011.10.008. PMID 22208608.